WO2003061723A1 - Balloons made from liquid crystal polymer blends - Google Patents

Balloons made from liquid crystal polymer blends Download PDF

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Publication number
WO2003061723A1
WO2003061723A1 PCT/US2003/001178 US0301178W WO03061723A1 WO 2003061723 A1 WO2003061723 A1 WO 2003061723A1 US 0301178 W US0301178 W US 0301178W WO 03061723 A1 WO03061723 A1 WO 03061723A1
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WO
WIPO (PCT)
Prior art keywords
polymer
liquid crystal
medical device
balloon
polyesterimide
Prior art date
Application number
PCT/US2003/001178
Other languages
French (fr)
Inventor
Lixiao Wang
Original Assignee
Scimed Life Systems, Inc
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Scimed Life Systems, Inc filed Critical Scimed Life Systems, Inc
Priority to DE60323935T priority Critical patent/DE60323935D1/en
Priority to CA002470191A priority patent/CA2470191A1/en
Priority to EP03731926A priority patent/EP1467776B1/en
Priority to JP2003561663A priority patent/JP2005515030A/en
Publication of WO2003061723A1 publication Critical patent/WO2003061723A1/en

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Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
    • A61L29/00—Materials for catheters, medical tubing, cannulae, or endoscopes or for coating catheters
    • A61L29/04—Macromolecular materials
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00—Stock material or miscellaneous articles
    • Y10T428/13—Hollow or container type article [e.g., tube, vase, etc.]
    • Y10T428/1352—Polymer or resin containing [i.e., natural or synthetic]
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00—Stock material or miscellaneous articles
    • Y10T428/13—Hollow or container type article [e.g., tube, vase, etc.]
    • Y10T428/1352—Polymer or resin containing [i.e., natural or synthetic]
    • Y10T428/139—Open-ended, self-supporting conduit, cylinder, or tube-type article
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00—Stock material or miscellaneous articles
    • Y10T428/13—Hollow or container type article [e.g., tube, vase, etc.]
    • Y10T428/1352—Polymer or resin containing [i.e., natural or synthetic]
    • Y10T428/139—Open-ended, self-supporting conduit, cylinder, or tube-type article
    • Y10T428/1393—Multilayer [continuous layer]

Definitions

  • the present invention relates to novel liquid crystal polymer blends for use in medical devices.
  • Catheter devices having a dilatation balloon mounted at the distal end of the catheter are useful in a variety of medical procedures.
  • a balloon reservoir may be used to deliver a biologically compatible fluid, such as radiologically opaque fluid for contrast x-rays, to a site within the body. Radial expansion of a balloon may be used to expand or inflate a stent positioned within the body.
  • a balloon may also be used to widen a vessel into which the catheter is inserted by dilating the blocked vessel. For example, in the technique of balloon angioplasty, a catheter is inserted for long distances into blood vessels of extremely reduced diameter and used to release or dilate stenoses therein by balloon inflation. These applications require thin walled high strength relatively inelastic balloons of accurately predictable inflation properties.
  • Balloon angioplasty has perhaps the most demanding requirements for such balloons.
  • this application requires that the balloons have uniformly thin walls and a small diameter in their unexpanded state.
  • the walls and waist thicknesses of the balloon limit the minimum diameter of the catheter distal end, and therefore determine the limits on minimum blood vessel diameter treatable by this method, as well as the ease of passage of the catheter through the vascular system.
  • the present invention relates to the use of melt blending novel polyesterimide anhydride liquid crystal polymers (LCP-PA) with various other polymeric materials for use in catheter devices.
  • LCP-PA polyesterimide anhydride liquid crystal polymers
  • the polyesterimide anhydride liquid crystal polymers have terminal and/or lateral anhydride groups.
  • the LCA-PA is melt blended with a polyester, a polyamide, a copolymer thereof or a mixture thereof.
  • the mixture is suitable for use in making extruded tubular structures for use in portions of medical devices such as catheter shafts, dilatation balloons, and so forth.
  • Fig. 1 is a side view of a catheter balloon according to the present invention.
  • Fig. 2 is a side view of a dual layer dilatation balloon according to the present invention.
  • Fig. 3 is a side view of a tubular structure according to the present invention.
  • the present invention relates to polymeric blends which include at least one liquid crystal polymer which is a polyesterimide anhydride (LCP-PA) and at least one other non-LCP base polymer.
  • the polymeric blends are melt blended and include from about 0.1 wt-% to about 40 wt-% of the LCP-PA, suitably about 0.2 wt- % to about 20 wt-%, and most suitably about 0.5 wt-% to about 10 wt-% of the LCP- PA and from about 60 wt-% to about 99.9 wt-% of at least one second polymer, hereinafter referred to as a base polymer, which is not a liquid crystal polymer, suitably about 80 wt-% to about 99.8 wt-% and most suitably about 90 wt-% to about 99.5 wt-% of at least one base polymer.
  • LCP-PA polyesterimide anhydride
  • the liquid crystal polymers (LCPs) useful herein may be characterized as meltable, reactive LCPs capable of forming covalent links with another polymer when mixed at elevated temperatures such as in an extruder or high shear mixer.
  • the LCPs may be chemically characterized as polyesterimides having terminal and/or lateral anhydride groups (PCP-PA).
  • Polyesterimides having terminal anhydride groups may be prepared by reacting p-acetoxybenzoic acid (pAOBA), hydroquinone diacetate (HDAC), 6-(4- carboxyphthalimido)-n-hexanoic acid (CPIHA) and an excess of trimellitic acid anhydride (TMAA) which produces a polyesterimide having an anhydride group at each end.
  • pAOBA p-acetoxybenzoic acid
  • HDAC hydroquinone diacetate
  • CPIHA 6-(4- carboxyphthalimido)-n-hexanoic acid
  • TMAA trimellitic acid anhydride
  • a polyesterimide having lateral anhydride groups located along the polymer chain, as well as terminal anhydride groups may be prepared by using the condensation product of 6-(4-carboxyphthalimido)-n-hexanoic acid (CPIHA) and 3,6- diacetoxy phthalic acid-l,2-anhydride (DAPAA).
  • CPIHA 6-(4-carboxyphthalimido)-n-hexanoic acid
  • DAPAA 3,6- diacetoxy phthalic acid-l,2-anhydride
  • the resulting precondensate may then be used as a substitute for the 6-(4-carboxyphthalimido)-n-hexanoic acid.
  • Using the precondensate rather than CPIHA results in a polyesterimide having both terminal and lateral anhydride groups.
  • the number of resultant anhydride groups as well as the molecular weight of the final LCP-PA may be varied by altering the ratio of CPIHA monomer to DAPAA monomer.
  • the number of anhydride groups may be varied between about 4 and about 18 and molecular weight of about 30 kg/mol to about 80 kg/mol could be obtained.
  • the LCP-PA melts at a temperature of less than 275 °C, suitably less than 250 °C, and most suitably in the range of about 150 °C to 250 °C.
  • the LCP-PA may then be blended with various other polymeric materials to impart higher strength and resistance to shrinkage to base polymer materials which have greater flexibility, softness or elasticity.
  • polymeric materials with which the LCP-PA may be blended include, but are not limited to, polyamides, polyesters, nylons, and any copolymers thereof, as well as mixtures thereof.
  • the polymeric materials have melting temperatures between about 140 °C and about 275 °C.
  • the term "copolymer" shall be used to describe any polymeric material which is formed of two or more monomers.
  • polyester copolymers useful in balloon formation include, for instance, poly(ester-block-ether) polymers such as HYTREL® available from DuPont de Nemours & Co.; ARNITEL® available from DSM; poly(ester-block-ester) polymers such as RITEFLEX® available from Hoechst-Celanese; and poly(ester-block-amide) polymers such as PEBAX® available from Atofina Engineering Polymers Division, North America.
  • poly(ester-block-ether) polymers such as HYTREL® available from DuPont de Nemours & Co.
  • ARNITEL® available from DSM
  • poly(ester-block-ester) polymers such as RITEFLEX® available from Hoechst-Celanese
  • poly(ester-block-amide) polymers such as PEBAX® available from Atofina Engineering Polymers Division, North America.
  • Polyesters useful herein include the phthalate and naphthalate polyesters and copolyesters including, but not limited to polyalkylene terephthalates such as polyethylene terephthalate and polybutylene terephthalate; polyalkylene terephthalate/isophthalate copolyesters; polyalkylene naphthalate such as polyethylene naphthalate and polybutylene naphthalate; polyalkylene terephthalate/naphthalate copolyesters; and so forth.
  • polyalkylene terephthalates such as polyethylene terephthalate and polybutylene terephthalate
  • polyalkylene terephthalate/isophthalate copolyesters such as polyethylene naphthalate and polybutylene naphthalate
  • polyalkylene terephthalate/naphthalate copolyesters and so forth.
  • polyesters and copolyesters examples include polyethylene terephthalate homopolymers and copolymers such as copolyester Type T74 available from Hoechst Celanese; KODAR® A150 available from Eastman Kodak; polyesters available under the tradename of CLEARTUFF® such as CLEARTUFF® 8006 or TRAYTUFF® available from Shell Chemical Co.; and SELAR® PT available from DuPont de Nemours & Co.; PEN homopolymers and PEN/PET copolymers including, for example VITUF® SLX available from Shell Chemical, PEN homopolymer 14991 available from Eastman Chemical Co. and various PEN homopolymers and copolymers available from Teijin Ltd. in Tokyo, Japan under the designations TN8070, TN8060, TN8756T and TN8880N.
  • copolyester Type T74 available from Hoechst Celanese
  • KODAR® A150 available from Eastman Kodak
  • Examples of useful polyamides include, but are not limited to, nylons 11 and 12.
  • Particular balloon materials which are may be blended with the LCP- PA in accordance with the present invention include poly(ether-block-amides), such as PEBAX® 7033 or 7233; poly(ester-block-ethers) such as ARNITEL® EM 40; polyethylene terephthalate; and nylon.
  • poly(ether-block-amides) such as PEBAX® 7033 or 7233
  • poly(ester-block-ethers) such as ARNITEL® EM 40
  • polyethylene terephthalate polyethylene terephthalate
  • nylon nylon
  • the polyesterimide anhydride LCP polymers are capable of forming graft polymers when melt blended at elevated temperatures with polyesters and polyamides.
  • the LCP-PAs may react with certain types of base polymers such as polyesters, polyamides, and so forth, under the right conditions, to form graft polymers.
  • base polymers such as polyesters, polyamides, and so forth, under the right conditions.
  • graft polymers may form at elevated temperatures which are standard for extrusion. Extrusion temperatures are commonly in the range of 200 °C-250 °C or higher, although lower or higher temperatures may be employed as well.
  • graft polymers may form at any elevated temperature but the extent of formation of the graft may vary.
  • composition may include other optional ingredients known to those of skill in the art including other polymeric materials.
  • the resultant melt blended compositions may be employed in medical devices such as catheter assemblies.
  • the compositions may be employed for balloon formation or catheter shafts.
  • the melt blended composition is particularly suitable for use in dilatation balloons used for percutaneous transluminal angioplasty and other minimally invasive procedures.
  • the balloon diameter for such applications is typically from about 1.5 to about 30 mm, depending on the exact use.
  • the wall thickness of the balloon is typically between about 0.0002" and 0.0020".
  • the balloons of the invention may be either single layer balloons or they may be multilayer balloons.
  • the balloon material is substantially non- compliant, providing a radial expansion of less than about 5%, suitably less than about 4% when inflation pressure is increased from about 4 atm to about 10 atm.
  • Balloon formation may be carried out in any conventional manner with conventional extrusion and blowing techniques, but basically there are three major steps in the process which include extruding a tubular preform or parison, blow molding the balloon and annealing the balloon.
  • the preform may be axially stretched before it is blown.
  • the balloons may also be optionally oriented by what is referred to in the industry as machine orientation during extrusion as known in the art. Techniques for balloon formation are discussed in U.S. Patent No. 4,490,421 to Levy and in U.S. Patent no. 5,348,538 issued September 20, 1994 to Wang et al.
  • Fig. 1 illustrates generally at 10, a catheter having a balloon 14 formed of the melt blend product of the present invention and an elongated tube 12 which also may optionally be formed of the melt blend product of the present invention.
  • Fig. 2 illustrates an alternative embodiment of the present invention in which catheter balloon 20 is formed of a dual layer structure in which the inner layer 22 is formed of the melt blend product of the present invention and the outer layer 24 is formed of a different polymer material, for instance, a relatively soft elastomeric polymer such as poly(ester-block-ether), poly(ester-block-ester) or poly(ester-block- amide).
  • a relatively soft elastomeric polymer such as poly(ester-block-ether), poly(ester-block-ester) or poly(ester-block- amide).
  • Fig. 3 illustrates a tubular structure 15 formed of the melt blend product of the present invention which may be used as a catheter shaft, among others.

Abstract

A portion of a medical device formed from a melt blend of a polyesterimide anhydride liquid crystal polymer and at least one other polymer.

Description

BALLOONS MADE FROM LIQUID CRYSTAL POLYMER BLENDS
FIELD OF THE INVENTION
The present invention relates to novel liquid crystal polymer blends for use in medical devices.
BACKGROUND OF THE INVENTION
Catheter devices having a dilatation balloon mounted at the distal end of the catheter are useful in a variety of medical procedures. A balloon reservoir may be used to deliver a biologically compatible fluid, such as radiologically opaque fluid for contrast x-rays, to a site within the body. Radial expansion of a balloon may be used to expand or inflate a stent positioned within the body. A balloon may also be used to widen a vessel into which the catheter is inserted by dilating the blocked vessel. For example, in the technique of balloon angioplasty, a catheter is inserted for long distances into blood vessels of extremely reduced diameter and used to release or dilate stenoses therein by balloon inflation. These applications require thin walled high strength relatively inelastic balloons of accurately predictable inflation properties.
Depending on the intended use of the balloon and the size of the vessel into which the catheter is inserted, the requirements for strength and the size of the balloon vary widely. Balloon angioplasty has perhaps the most demanding requirements for such balloons. Typically, this application requires that the balloons have uniformly thin walls and a small diameter in their unexpanded state. The walls and waist thicknesses of the balloon limit the minimum diameter of the catheter distal end, and therefore determine the limits on minimum blood vessel diameter treatable by this method, as well as the ease of passage of the catheter through the vascular system.
Further requirements include high balloon strength which enables the balloon to push open a stenosis and to avoid bursting of the balloon under the high internal pressures necessary to inflate the balloon at the site of the stenosis. The balloon must also be sufficiently elastic to allow a surgeon to vary the diameter of the balloon as required to treat individual lesions. However, the balloon must have relatively low elasticity in order to accurately control the balloon diameter, and variations in pressure must not cause wide variations in balloon diameter. These physical requirements may conflict with one another and thus can make the formation of a balloon from a single material difficult depending on the end use of the balloon. Various approaches have been taken including melt blending materials and the use of multilayer balloon structures. Blends of liquid crystal polymers and thermoplastic non-LCP base polymers have been employed including polyesteramide and polyester-type LCPs, for example. See commonly assigned 6242063 and US 6284333.
SUMMARY OF THE INVENTION The present invention relates to the use of melt blending novel polyesterimide anhydride liquid crystal polymers (LCP-PA) with various other polymeric materials for use in catheter devices.
The polyesterimide anhydride liquid crystal polymers have terminal and/or lateral anhydride groups. In some embodiments, the LCA-PA is melt blended with a polyester, a polyamide, a copolymer thereof or a mixture thereof. The mixture is suitable for use in making extruded tubular structures for use in portions of medical devices such as catheter shafts, dilatation balloons, and so forth.
BRIEF DESCRIPTION OF THE DRAWINGS
Fig. 1 is a side view of a catheter balloon according to the present invention.
Fig. 2 is a side view of a dual layer dilatation balloon according to the present invention. Fig. 3 is a side view of a tubular structure according to the present invention.
DETAILED DESCRIPTIONS OF THE PREFERRED EMBODIMENTS
The present invention relates to polymeric blends which include at least one liquid crystal polymer which is a polyesterimide anhydride (LCP-PA) and at least one other non-LCP base polymer. The polymeric blends are melt blended and include from about 0.1 wt-% to about 40 wt-% of the LCP-PA, suitably about 0.2 wt- % to about 20 wt-%, and most suitably about 0.5 wt-% to about 10 wt-% of the LCP- PA and from about 60 wt-% to about 99.9 wt-% of at least one second polymer, hereinafter referred to as a base polymer, which is not a liquid crystal polymer, suitably about 80 wt-% to about 99.8 wt-% and most suitably about 90 wt-% to about 99.5 wt-% of at least one base polymer.
The liquid crystal polymers (LCPs) useful herein may be characterized as meltable, reactive LCPs capable of forming covalent links with another polymer when mixed at elevated temperatures such as in an extruder or high shear mixer. The LCPs may be chemically characterized as polyesterimides having terminal and/or lateral anhydride groups (PCP-PA).
Polyesterimides having terminal anhydride groups may be prepared by reacting p-acetoxybenzoic acid (pAOBA), hydroquinone diacetate (HDAC), 6-(4- carboxyphthalimido)-n-hexanoic acid (CPIHA) and an excess of trimellitic acid anhydride (TMAA) which produces a polyesterimide having an anhydride group at each end.
A polyesterimide having lateral anhydride groups located along the polymer chain, as well as terminal anhydride groups, may be prepared by using the condensation product of 6-(4-carboxyphthalimido)-n-hexanoic acid (CPIHA) and 3,6- diacetoxy phthalic acid-l,2-anhydride (DAPAA). The resulting precondensate may then be used as a substitute for the 6-(4-carboxyphthalimido)-n-hexanoic acid. Using the precondensate rather than CPIHA results in a polyesterimide having both terminal and lateral anhydride groups.
The number of resultant anhydride groups as well as the molecular weight of the final LCP-PA may be varied by altering the ratio of CPIHA monomer to DAPAA monomer. The number of anhydride groups may be varied between about 4 and about 18 and molecular weight of about 30 kg/mol to about 80 kg/mol could be obtained. Suitably, the LCP-PA melts at a temperature of less than 275 °C, suitably less than 250 °C, and most suitably in the range of about 150 °C to 250 °C.
The LCP-PA may then be blended with various other polymeric materials to impart higher strength and resistance to shrinkage to base polymer materials which have greater flexibility, softness or elasticity. Examples of polymeric materials with which the LCP-PA may be blended include, but are not limited to, polyamides, polyesters, nylons, and any copolymers thereof, as well as mixtures thereof. Suitably, the polymeric materials have melting temperatures between about 140 °C and about 275 °C. As used herein, the term "copolymer" shall be used to describe any polymeric material which is formed of two or more monomers.
Some specific examples of commercially available polyester copolymers useful in balloon formation include, for instance, poly(ester-block-ether) polymers such as HYTREL® available from DuPont de Nemours & Co.; ARNITEL® available from DSM; poly(ester-block-ester) polymers such as RITEFLEX® available from Hoechst-Celanese; and poly(ester-block-amide) polymers such as PEBAX® available from Atofina Engineering Polymers Division, North America. Polyesters useful herein include the phthalate and naphthalate polyesters and copolyesters including, but not limited to polyalkylene terephthalates such as polyethylene terephthalate and polybutylene terephthalate; polyalkylene terephthalate/isophthalate copolyesters; polyalkylene naphthalate such as polyethylene naphthalate and polybutylene naphthalate; polyalkylene terephthalate/naphthalate copolyesters; and so forth. Examples of commercially available polyesters and copolyesters include polyethylene terephthalate homopolymers and copolymers such as copolyester Type T74 available from Hoechst Celanese; KODAR® A150 available from Eastman Kodak; polyesters available under the tradename of CLEARTUFF® such as CLEARTUFF® 8006 or TRAYTUFF® available from Shell Chemical Co.; and SELAR® PT available from DuPont de Nemours & Co.; PEN homopolymers and PEN/PET copolymers including, for example VITUF® SLX available from Shell Chemical, PEN homopolymer 14991 available from Eastman Chemical Co. and various PEN homopolymers and copolymers available from Teijin Ltd. in Tokyo, Japan under the designations TN8070, TN8060, TN8756T and TN8880N.
Examples of useful polyamides include, but are not limited to, nylons 11 and 12.
Particular balloon materials which are may be blended with the LCP- PA in accordance with the present invention include poly(ether-block-amides), such as PEBAX® 7033 or 7233; poly(ester-block-ethers) such as ARNITEL® EM 40; polyethylene terephthalate; and nylon. The formation of catheter balloons made of block copolymer elastomers where the hard segments are polyester or polyamide and the soft segments are polyether, is discussed in U.S. Patent No. 5,556,383 issued September 17, 1996 to Wang et al. incorporated by reference herein.
The polyesterimide anhydride LCP polymers are capable of forming graft polymers when melt blended at elevated temperatures with polyesters and polyamides. The LCP-PAs may react with certain types of base polymers such as polyesters, polyamides, and so forth, under the right conditions, to form graft polymers. For instance, at elevated temperatures which are standard for extrusion, graft polymers may form. Extrusion temperatures are commonly in the range of 200 °C-250 °C or higher, although lower or higher temperatures may be employed as well. Furthermore, graft polymers may form at any elevated temperature but the extent of formation of the graft may vary.
Additionally, the composition may include other optional ingredients known to those of skill in the art including other polymeric materials.
The resultant melt blended compositions may be employed in medical devices such as catheter assemblies. In particular, the compositions may be employed for balloon formation or catheter shafts.
The melt blended composition is particularly suitable for use in dilatation balloons used for percutaneous transluminal angioplasty and other minimally invasive procedures. The balloon diameter for such applications is typically from about 1.5 to about 30 mm, depending on the exact use. The wall thickness of the balloon is typically between about 0.0002" and 0.0020".
The balloons of the invention may be either single layer balloons or they may be multilayer balloons.
In one embodiment, the balloon material is substantially non- compliant, providing a radial expansion of less than about 5%, suitably less than about 4% when inflation pressure is increased from about 4 atm to about 10 atm.
Balloon formation may be carried out in any conventional manner with conventional extrusion and blowing techniques, but basically there are three major steps in the process which include extruding a tubular preform or parison, blow molding the balloon and annealing the balloon. Depending on the balloon material employed, the preform may be axially stretched before it is blown. The balloons may also be optionally oriented by what is referred to in the industry as machine orientation during extrusion as known in the art. Techniques for balloon formation are discussed in U.S. Patent No. 4,490,421 to Levy and in U.S. Patent no. 5,348,538 issued September 20, 1994 to Wang et al.
Fig. 1 illustrates generally at 10, a catheter having a balloon 14 formed of the melt blend product of the present invention and an elongated tube 12 which also may optionally be formed of the melt blend product of the present invention.
Fig. 2 illustrates an alternative embodiment of the present invention in which catheter balloon 20 is formed of a dual layer structure in which the inner layer 22 is formed of the melt blend product of the present invention and the outer layer 24 is formed of a different polymer material, for instance, a relatively soft elastomeric polymer such as poly(ester-block-ether), poly(ester-block-ester) or poly(ester-block- amide).
The present invention may be of course used for the extrusion of any tubular structures useful in medical devices. Fig. 3 illustrates a tubular structure 15 formed of the melt blend product of the present invention which may be used as a catheter shaft, among others.
The above disclosure is not exhaustive and is intended for illustrative purposes only and thus is not intended to limit the scope of the present invention. This description will suggest many variations and alternatives to one of ordinary skill in this art. Those familiar with the art may recognize other equivalents to the specific embodiments described herein which equivalents are also intended to be encompassed by the claims.

Claims

CLAIMS:
1. A medical device at least a portion of which is composed of a polymeric material which is a melt blend product comprising: a) at least one polyesterimide anhydride liquid crystal polymer; and b) at least one base polymer.
2. The medical device of claim 1 wherein said polyesterimide anhydride liquid crystal polymer has terminal and lateral anhydride groups.
3. The medical device of claim 1 wherein said polyesterimide anhydride liquid crystal polymer has about 4 to about 18 anhydride groups per molecule.
4. The medical device of claim 1 wherein said at least one base polymer is a polyamide, a polyester, a copolymer thereof, or mixture thereof.
5. The medical device of claim 1 wherein said at least one base polymer is a poly(ether-block-amide), a poly(ester-block-ether), a polyethyleneterephthalate, nylon 11, nylon 12, or mixture thereof.
6. The medical device of claim 1 wherein said polyesterimide anhydride liquid crystal polymer and said at least one base polymer react to form a graft polymer.
7. The medical device of claim 1 wherein said medical device is a catheter.
8. The medical device of claim 1 wherein said portion of said medical device is a balloon mounted on a catheter.
9. The medical device of claim 1 wherein said portion of said medical device is a catheter shaft.
10. The dilatation balloon of claim 1 wherein said melt blend product comprises about 0.1 wt-% to about 40 wt-% of said liquid crystal polymer and about 60 wt-%) to about 99.9 wt-% of at least one other polymer.
11. The dilatation balloon of claim 1 wherein said melt blend product comprises about 0.5 wt-% to about 10 wt-% of said liquid crystal polymer and about 90 wt-% to about 99.5 wt-% of at least one other polymer.
12. A dilatation balloon formed from an extruded tubular parison which is a melt blend product of at least one polyesterimide anhydride liquid crystal polymer and at least one other polymer.
13. The dilatation balloon of claim 12 wherein said polyesterimide has terminal and lateral anhydride groups.
14. The dilatation balloon of claim 12 wherein said at least one other polymer is a polyester, a polyamide, a copolymer thereof or a mixture thereof.
15. The dilatation balloon of claim 12 wherein said at least one other polymer is a poly(ester-block-ether), a poly(ether-block-amide), polyethyleneterephthalate, nylon 11, nylon 12, or mixture thereof.
16. The dilatation balloon of claim 12 wherein said polyesterimide anhydride liquid crystal polymer and at least one other polymer form a graft polymer.
17. The dilatation balloon of claim 12 wherein said melt blend product comprises about 0.1 wt-%) to about 40 wt-% of said polyesterimide anhydride liquid crystal polymer and about 60 wt-% to about 99.9 wt-% of at least one other polymer.
18. The dilatation balloon of claim 12 wherein said melt blend product comprises about 0.5 wt-% to about 10 wt-% of said polyesterimide anhydride liquid crystal polymer and about 90 wt-% to about 99.5 wt-% of at least one other polymer.
19. The dilatation balloon of claim 12 wherein said polyesterimide anhydride has about 4 to about 18 anhydride groups per molecule.
20. A process of making a dilatation balloon comprising the steps of melt blending polyesterimide anhydride liquid crystal polymer and at least one other polymer in an extruder at a temperature of about 140 °C and 275 °C to form a tubular parison and blow molding said tubular parison to form a dilatation balloon.
21. The process of claim 20 wherein said at least one other polymer is a polyester, a polyamide, a copolymer thereof, or mixture thereof.
22. The process of claim 20 further comprising the step of orienting said balloon.
PCT/US2003/001178 2002-01-23 2003-01-15 Balloons made from liquid crystal polymer blends WO2003061723A1 (en)

Priority Applications (4)

Application Number Priority Date Filing Date Title
DE60323935T DE60323935D1 (en) 2002-01-23 2003-01-15 BALLONS MADE FROM LIQUID CRYSTAL POLYMER MIXTURES
CA002470191A CA2470191A1 (en) 2002-01-23 2003-01-15 Balloons made from liquid crystal polymer blends
EP03731926A EP1467776B1 (en) 2002-01-23 2003-01-15 Balloons made from liquid crystal polymer blends
JP2003561663A JP2005515030A (en) 2002-01-23 2003-01-15 Balloon formed from liquid crystal polymer blend

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US10/055,585 2002-01-23
US10/055,585 US6730377B2 (en) 2002-01-23 2002-01-23 Balloons made from liquid crystal polymer blends

Publications (1)

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WO2003061723A1 true WO2003061723A1 (en) 2003-07-31

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DE60323935D1 (en) 2008-11-20
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EP2008674B1 (en) 2012-03-14
EP2008674A1 (en) 2008-12-31
CA2470191A1 (en) 2003-07-31
US20030138577A1 (en) 2003-07-24
ES2311707T3 (en) 2009-02-16
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EP1467776B1 (en) 2008-10-08
US6730377B2 (en) 2004-05-04

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